Canonical Allele Identifier: CA2246126522

Gene: ALOX12B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8076380G= , CM000679.2:g.8076380G=	GRCh38
NC_000017.10:g.7979698G= , CM000679.1:g.7979698G=	GRCh37
NC_000017.9:g.7920423G=	NCBI36
NG_007099.1:g.16324C=
NG_007099.2:g.16337C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647874.1:c.1363-36C= MANE Select	ENSP00000497784.1:n.1363-36C=
ENST00000649809.1:c.427-36C=	ENSP00000496845.1:n.427-36C=
ENST00000319144.4:c.1363-36C=	ENSP00000315167.4:n.1363-36C=
ENST00000577351.5:n.310-36C=
ENST00000583276.5:n.747-36C=
ENST00000584116.1:n.619-36C=
NM_001139.2:c.1363-36C=	NP_001130.1:n.1363-36C=
NM_001139.3:c.1363-36C= MANE Select	NP_001130.1:n.1363-36C=